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52. Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report

53. Molecular and Phenotypic Characterization of the RORB-Related Disorder

54. GRM7-related disorder: Five additional patients from three independent families and review of the literature

55. Paul trapping of radioactive 6He+ions and direct observation of their beta-decay

56. Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder

60. GRIN1 variants associated with neurodevelopmental disorders reveal channel gating pathomechanisms

62. Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital

65. Nanobeacon: A time calibration device for the KM3NeT neutrino telescope

67. Transposable element expression with variation in sex chromosome number supports a toxic Y effect on human longevity

68. Asparagine synthetase deficiency: A novel case with an unusual molecular mechanism

69. Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature

70. The KM3NeT multi-PMT optical module

71. KM3NeT broadcast optical data transport system

74. Site Isolation in Metal–Organic Layers Enhances Photoredox Gold Catalysis

75. Implementation and first results of the KM3NeT real-time core-collapse supernova neutrino search

76. A genome-wide DNA methylation signature for SETD1B-related syndrome

77. Probing invisible neutrino decay with KM3NeT-ORCA

78. The Power Board of the KM3NeT Digital Optical Module: design, upgrade, and production

79. Molecular and Phenotypic Characterization of the RORB-Related Disorder.

81. First observation of the cosmic ray shadow of the Moon and the Sun with KM3NeT/ORCA

82. Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA

83. Deconvolution methods used for the development of a neutron spectrometer

84. Molecular characterization of a cohort of 73 patients with infantile spasms syndrome

85. Targeted next‐generation sequencing in a large series of fetuses with severe renal diseases

86. Application of a new spectral deconvolution method for in vitro dosimetry in assessment of targeted alpha therapy

88. Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing

91. KM3NeT broadcast optical data transport system

92. Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing

93. Performance of the reconstruction algorithms of the FIRST experiment pixel sensors vertex detector

94. Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7

96. In vitro dosimetry for assessment of Targeted-Alpha-Therapy

97. First observation of the cosmic ray shadow of the Moon and the Sun with KM3NeT/ORCA

98. Atmospheric neutrinos with the first KM3NeT/ORCA data and prospects for measuring the atmospheric neutrino flux

99. Muon bundle reconstruction with KM3NeT/ORCA using graph convolutional networks

100. Expectations for the high-energy neutrino detection from starburst galaxies with KM3NeT/ARCA

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